Literature DB >> 16874104

Cellular autophagy machinery is not required for vaccinia virus replication and maturation.

Haiyan Zhang1, Claude E Monken, Yong Zhang, John Lenard, Noboru Mizushima, Edmund C Lattime, Shengkan Jin.   

Abstract

The origin of the primary membrane of the vaccinia virus, a double-membrane structure that surrounds the immature virions (IV), is not fully understood. Here we investigated whether the primary membrane originates from the autophagic membrane. Morphologic studies by electron microscopy (EM) showed no apparent difference in viral maturation in the autophagy-deficient cell lines, the atg5(-/-) mouse embryonic fibroblasts (MEFs) and the beclin1(-/-) embryonic stem (ES) cells, compared to their isogenic wild-type counterparts. Moreover, viral growth curves demonstrated that vaccinia viruses replicate and mature in the autophagy-deficient cell lines as efficiently as they do in their isogenic wild type counterpart cells. This study indicates that the cellular autophagy machinery is not required for the life-cycle of vaccinia virus, suggesting that the primary vaccinia viral membrane does not originate from the autophagic membrane.

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Year:  2006        PMID: 16874104     DOI: 10.4161/auto.2.2.2297

Source DB:  PubMed          Journal:  Autophagy        ISSN: 1554-8627            Impact factor:   16.016


  21 in total

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Review 2.  Viruses and autophagy.

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4.  mTOR Dysregulation by Vaccinia Virus F17 Controls Multiple Processes with Varying Roles in Infection.

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5.  Inhibition of ULK1 and Beclin1 by an α-herpesvirus Akt-like Ser/Thr kinase limits autophagy to stimulate virus replication.

Authors:  Rosa M Rubio; Ian Mohr
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Journal:  Cell Rep       Date:  2016-10-18       Impact factor: 9.423

Review 7.  Autophagy, antiviral immunity, and viral countermeasures.

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Journal:  Biochim Biophys Acta       Date:  2009-03-02

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Review 9.  Autophagy and viruses: adversaries or allies?

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Review 10.  Eating the enemy within: autophagy in infectious diseases.

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